Warning
Linkbio Corp. Recalls LinkBio CORE Workstation
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-1810-2026Medical Device
Linkbio Corp. Recalls LinkBio CORE Workstation
Linkbio Corp. · Class II — Moderate Risk
Product Description
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Reason for Recall
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide distribution in the state of Alabama, Florida, and Kansas.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a medical device from Linkbio Corp., initiated on March 12, 2026. The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen. This recall covers 5 units, distributed nationwide. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.